Department of Clinical Pharmacology and Toxicology, University Hospital Zurich, Zurich, Switzerland.
Am J Physiol Gastrointest Liver Physiol. 2012 Jan 1;302(1):G123-33. doi: 10.1152/ajpgi.00102.2011. Epub 2011 Oct 20.
The apical sodium-dependent bile acid transporter (ASBT) is expressed abundantly in the ileum and mediates bile acid absorption across the apical membranes. Caudal-type homeobox proteins CDX1 and CDX2 are transcription factors that regulate genes involved in intestinal epithelial differentiation and proliferation. Aberrant expression of both ASBT and CDXs in Barrett's esophagus (BE) prompted us to study, whether the expression of the ASBT gene is regulated by CDXs. Short interfering RNA-mediated knockdown of CDXs resulted in reduced ASBT mRNA expression in intestinal cells. CDXs strongly induced the activity of the ASBT promoter in reporter assays in esophageal and intestinal cells. Nine CDX binding sites were predicted in silico within the ASBT promoter, and binding of CDXs to six of them was verified in vitro and within living cells by electrophoretic mobility shift assays and chromatin immunoprecipitation assays, respectively. RNAs were extracted from esophageal biopsies from 20 BE patients and analyzed by real-time PCR. Correlation with ASBT expression was found for CDX1, CDX2, and HNF-1α in BE biopsies. In conclusion, the human ASBT promoter is activated transcriptionally by CDX1 and CDX2. Our finding provides a possible explanation for the reported observation that ASBT is aberrantly expressed in esophageal metaplasia that also expresses CDX transcription factors.
顶端钠依赖性胆汁酸转运体(ASBT)在回肠中大量表达,并介导胆汁酸穿过顶膜的吸收。尾型同源盒蛋白 CDX1 和 CDX2 是调节肠上皮分化和增殖相关基因的转录因子。巴雷特食管(BE)中 ASBT 和 CDXs 的异常表达促使我们研究 ASBT 基因的表达是否受 CDXs 调节。CDXs 的短发夹 RNA 介导的敲低导致肠细胞中 ASBT mRNA 表达减少。在食管和肠细胞中的报告基因实验中,CDXs 强烈诱导 ASBT 启动子的活性。在 ASBT 启动子内,计算机预测了 9 个 CDX 结合位点,通过电泳迁移率变动分析和染色质免疫沉淀分析,分别在体外和活细胞中验证了 CDXs 对其中 6 个结合位点的结合。从 20 例 BE 患者的食管活检中提取 RNA,并用实时 PCR 进行分析。在 BE 活检中发现 CDX1、CDX2 和 HNF-1α 与 ASBT 表达相关。总之,人 ASBT 启动子被 CDX1 和 CDX2 转录激活。我们的发现为 ASBT 在表达 CDX 转录因子的食管化生中异常表达的报道提供了可能的解释。